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Whole Body Vibration Exercise Training for Institutionalized Elderly

T

The Hong Kong Polytechnic University

Status

Unknown

Conditions

Geriatric Disorder

Treatments

Device: Whole body vibration
Behavioral: Conventional exercise
Behavioral: Control

Study type

Interventional

Funder types

Other

Identifiers

NCT01735682
HSEARS20120730001

Details and patient eligibility

About

It is hypothesized that whole body vibration exercise group will have significantly more improvement in physical functioning and reduction in fall incidence among institutionalized elderly, compared with conventional exercise group and control group.

Enrollment

68 estimated patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Functional Ambulation Category 1 to 4
  • able to understand simple verbal commands
  • able to tolerate intermittent physical activity for at least 45 minutes
  • able to perform knee flexion >45 degree
  • able to stand with or without support for 1 minute or more

Exclusion criteria

  • peripheral vascular disease
  • any symptoms associated with vestibular disorder
  • any contraindications to exercise (e.g. unstable angina)
  • any serious illnesses that preclude participation (e.g. cancer)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

68 participants in 3 patient groups

Whole body vibration
Experimental group
Description:
This group will receive whole body vibration and conventional exercise training (1 hour per session, 3 sessions per week, for 8 consecutive weeks).
Treatment:
Device: Whole body vibration
Conventional exercise
Active Comparator group
Description:
This group will receive convention exercise training (1 hour per session, 3 sessions per week, for 8 consecutive weeks).
Treatment:
Behavioral: Conventional exercise
Control
Active Comparator group
Description:
This group will have exercise training that involve only the upper limbs (about 30 minutes per session, 3 sessions per week, for 8 consecutive weeks).
Treatment:
Behavioral: Control

Trial contacts and locations

1

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Central trial contact

Philip Chan, MSc

Data sourced from clinicaltrials.gov

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